聚酰胺
膜
纳滤
薄膜复合膜
基质(水族馆)
材料科学
复合材料
磁导率
薄膜
化学工程
反渗透
化学
纳米技术
工程类
地质学
生物化学
海洋学
作者
Senlin Shao,Jun Xing,Hongting Wan,Jiajia Lu,Li Long,Ruijun Zhang,Hao Guo,Chuyang Y. Tang
标识
DOI:10.1021/acs.est.5c08645
摘要
Thin-film composite (TFC) nanofiltration (NF) membranes are widely used in water treatment and resource recovery. Researchers generally take for granted that the dense polyamide rejection film dictates the overall hydraulic resistance of these membranes, neglecting the contributions of the substrate and the transverse transport of water to reach substrate pores. To address this critical gap, we developed a resistance-in-series model to quantify the resistances from the polyamide film, substrate, and transverse transport. Calibration with multiple experimental data sets revealed that the polyamide film resistance varied over a wide range of 2.90 × 1012 to 40.15 × 1012 m-1, strongly correlating to film thicknesses (correlation coefficients >0.95), with a thickness-normalized resistance of (0.44 ± 0.12) × 1012 m-1 nm-1. Contrarily, the intrinsic water permeability of polyamide material showed less variation (0.53 × 103 to 1.56 × 103 LMH bar-1 nm). Contrary to common belief, both the substrate and transverse transport contributed significant resistances of (2.4 ± 1.3) × 1012 and 5 × 1012 m-1, respectively. These two resistances became particularly non-negligible for membranes with thinner polyamide films. Our study provides the first detailed quantitative analysis of key contributors to hydraulic resistance and provides valuable insights for high-permeable NF membranes.
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